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Hematopoietic stem cell transplantation for adolescents and adults with inborn errors of immunity: an EBMT IEWP study

医学 造血干细胞移植 单变量分析 内科学 移植 支气管扩张 免疫抑制 脾切除术 儿科 外科 多元分析 脾脏
作者
Michael H. Albert,Tiarlan Sirait,Dirk-Jan Eikema,Katerina Bakunina,Claudia Wehr,Felipe Suárez,María Laura Fox,Nizar Mahlaoui,Andrew R. Gennery,Arjan C. Lankester,Rita Beier,Maria Ester Bernardo,Venetia Bigley,Caroline A. Lindemans,Siobhan O. Burns,Ben Carpenter,Jarosław Dybko,Tayfun Güngör,Fabian Hauck,Su Han Lum,Dmitry Balashov,Roland Meisel,Despina Moshous,Ansgar Schulz,Carsten Speckmann,Mary Slatter,Brigitte Strahm,Duygu Uçkan,Isabelle Meyts,Tanja C. Vallée,Robert Wynn,Bénédicte Neven,Emma Morris,Alessandro Aiuti,Alexei Maschan,Mahmoud Aljurf,Tobias Gedde‐Dahl,Günhan Gürman,Victoria Bordon,Gergely Kriván,Franco Locatelli,Fulvio Porta,David Valcárcel,Yves Béguin,Maura Faraci,Nicolaus Kröger,Alexander Kulagin,Peter J. Shaw,Hendrik Veelken,Cristina Díaz de Heredia,Franca Fagioli,Matthias Felber,Bernd Gruhn,Wolfgang Holter,Claudia Rössig,Petr Sedláček,Jane Apperley,Mouhab Ayas,Ivana Boďová,Goda Choi,Jan J. Cornelissen,Anne Sîrvent,Anjum Khan,Alphan Küpesiz,Stig Lenhoff,Hakan Özdoğu,Nicolas von der Weid,Montserrat Rovira,Rik Schots,Donald C. Vinh
出处
期刊:Blood [Elsevier BV]
卷期号:140 (14): 1635-1649 被引量:33
标识
DOI:10.1182/blood.2022015506
摘要

Allogeneic hematopoietic stem cell transplantation (HSCT) is the gold standard curative therapy for infants and children with many inborn errors of immunity (IEI), but adolescents and adults with IEI are rarely referred for transplant. Lack of published HSCT outcome data outside small, single-center studies and perceived high risk of transplant-related mortality have delayed the adoption of HSCT for IEI patients presenting or developing significant organ damage later in life. This large retrospective, multicenter HSCT outcome study reports on 329 IEI patients (age range, 15-62.5 years at HSCT). Patients underwent first HSCT between 2000 and 2019. Primary endpoints were overall survival (OS) and event-free survival (EFS). We also evaluated the influence of IEI-subgroup and IEI-specific risk factors at HSCT, including infections, bronchiectasis, colitis, malignancy, inflammatory lung disease, splenectomy, hepatic dysfunction, and systemic immunosuppression. At a median follow-up of 44.3 months, the estimated OS at 1 and 5 years post-HSCT for all patients was 78% and 71%, and EFS was 65% and 62%, respectively, with low rates of severe acute (8%) or extensive chronic (7%) graft-versus-host disease. On univariate analysis, OS and EFS were inferior in patients with primary antibody deficiency, bronchiectasis, prior splenectomy, hepatic comorbidity, and higher hematopoietic cell transplant comorbidity index scores. On multivariable analysis, EFS was inferior in those with a higher number of IEI-associated complications. Neither age nor donor had a significant effect on OS or EFS. We have identified age-independent risk factors for adverse outcome, providing much needed evidence to identify which patients are most likely to benefit from HSCT.
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